Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Minimal residual disease (MRD) is now a powerful surrogate marker to assess the response to chemotherapy in acute myeloid leukemia (AML). mutation has been associated with adverse outcomes. In this study, we aimed to investigate the impact of status on NPM1 MRD predictive value for survival in a retrospective cohort of AML patients aged over 60 years old treated intensively. A total of 138 patients treated for -mutated AML in two French institutions were analyzed retrospectively. status did not influence the probability of having a ≥ 4log MRD1 reduction after induction. Only 20.4% of patients reached ≥ 4log MRD1 reduction compared to 47.5% in wt cases. A 4log reduction of MRD was associated with a better outcome, even in mutated patients, independent of the allelic ratio. negative patients who reached a 4log reduction had a superior outcome to those who did not (HR = 0.23; < 0.001). However, postinduction MRD1 reduction was not predictive of OS and LFS in mut patients. These results confirm that post-induction MRD1 is a reliable tool to assess disease outcome in elderly AML patients. However, the presence of also identifies a subgroup of patients at high risk of relapse.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124973 | PMC |
http://dx.doi.org/10.3390/cancers13092156 | DOI Listing |
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